Exacerbation Rate in Generalized Myasthenia Gravis and Its Predictors. Abuzinadah, A., R., Alanazy, M., H., Butt, N., S., Barohn, R., J., & Dimachkie, M., M. European Neurology, 83(6):1-6, S. Karger AG, 12, 2020.
Exacerbation Rate in Generalized Myasthenia Gravis and Its Predictors [link]Website  abstract   bibtex   

<b><i>Objective:</i></b> The aim of the study was to estimate the exacerbation incidence rate (IR) in acetylcholine receptor antibody (AChR)-positive generalized myasthenia gravis (MG) and its predictors. <b><i>Methods:</i></b> The primary outcome in this retrospective study was to estimate moderate-to-severe (M-S) exacerbations IR in the early course of generalized MG. The secondary outcome was to explore the predictors of MG exacerbations. <b><i>Results:</i></b> Between 1999 and 2015, we identified 78 AChR-positive generalized MG patients and 37 M-S exacerbations over the first 6 years following the onset of generalized MG symptoms. The M-S exacerbation IR was 12.2 per 100 person years (95% confidence interval [CI] 8.8–16.8). Any exacerbation (including mild) IR was 24.4 per 100 person years (95% CI 19.4–30.7). After controlling for confounding factors, MG exacerbation IR predictors included gender, disease severity at onset, and prednisone dose reduction with risk ratio of 0.34 (male gender), 2.67, and 20.8, respectively (all <i>p</i> values &#x3c;0.05). M-S exacerbation occurred in 25 cases (32.1%), while any exacerbation (mild or M-S) was detected in 45 cases (57.7%). <b><i>Conclusion:</i></b> More than half of newly diagnosed AChR + MG cases experience an exacerbation in the first 6 years. Gender, disease severity at onset and prednisone dose reduction are predictors that could inform clinical practice and future research.

@article{
 title = {Exacerbation Rate in Generalized Myasthenia Gravis and Its Predictors},
 type = {article},
 year = {2020},
 identifiers = {[object Object]},
 keywords = {Exacerbation,Immunosuppressant,Incidence,Myasthenia gravis,Predictors,Prednisone},
 pages = {1-6},
 volume = {83},
 websites = {https://www.karger.com/Article/FullText/512077},
 month = {12},
 publisher = {S. Karger AG},
 day = {15},
 id = {a2631a1d-9dce-3f03-8b2c-6f790f0ac058},
 created = {2021-01-20T10:16:08.692Z},
 accessed = {2021-01-20},
 file_attached = {false},
 profile_id = {49efd9d1-b84a-3562-b8db-36e64ac7ba81},
 last_modified = {2021-01-20T10:16:08.692Z},
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 abstract = {<p>&lt;b&gt;&lt;i&gt;Objective:&lt;/i&gt;&lt;/b&gt; The aim of the study was to estimate the exacerbation incidence rate (IR) in acetylcholine receptor antibody (AChR)-positive generalized myasthenia gravis (MG) and its predictors. &lt;b&gt;&lt;i&gt;Methods:&lt;/i&gt;&lt;/b&gt; The primary outcome in this retrospective study was to estimate moderate-to-severe (M-S) exacerbations IR in the early course of generalized MG. The secondary outcome was to explore the predictors of MG exacerbations. &lt;b&gt;&lt;i&gt;Results:&lt;/i&gt;&lt;/b&gt; Between 1999 and 2015, we identified 78 AChR-positive generalized MG patients and 37 M-S exacerbations over the first 6 years following the onset of generalized MG symptoms. The M-S exacerbation IR was 12.2 per 100 person years (95% confidence interval [CI] 8.8–16.8). Any exacerbation (including mild) IR was 24.4 per 100 person years (95% CI 19.4–30.7). After controlling for confounding factors, MG exacerbation IR predictors included gender, disease severity at onset, and prednisone dose reduction with risk ratio of 0.34 (male gender), 2.67, and 20.8, respectively (all &lt;i&gt;p&lt;/i&gt; values &amp;#x3c;0.05). M-S exacerbation occurred in 25 cases (32.1%), while any exacerbation (mild or M-S) was detected in 45 cases (57.7%). &lt;b&gt;&lt;i&gt;Conclusion:&lt;/i&gt;&lt;/b&gt; More than half of newly diagnosed AChR + MG cases experience an exacerbation in the first 6 years. Gender, disease severity at onset and prednisone dose reduction are predictors that could inform clinical practice and future research.</p>},
 bibtype = {article},
 author = {Abuzinadah, Ahmad R. and Alanazy, Mohammed H. and Butt, Nadeem S. and Barohn, Richard J. and Dimachkie, Mazen M.},
 journal = {European Neurology},
 number = {6}
}

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